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D-NAP 预防性治疗肌萎缩侧索硬化症 SOD 突变小鼠模型:tau 病的发现和治疗综述。

D-NAP prophylactic treatment in the SOD mutant mouse model of amyotrophic lateral sclerosis: review of discovery and treatment of tauopathy.

机构信息

Department of Human Molecular Genetics and Biochemistry, Sagol School of Neuroscience, Adams Super Center for Brain Studies, Tel Aviv University, Tel Aviv, Israel.

出版信息

J Mol Neurosci. 2012 Nov;48(3):597-602. doi: 10.1007/s12031-012-9882-6.

Abstract

Davunetide (NAP) is a leading drug candidate being tested against tauopathy. Davunetide is an eight-amino-acid peptide fragment derived by structure-activity studies from activity-dependent neuroprotective protein, activity-dependent neuroprotective protein (ADNP). ADNP is essential for brain formation. ADNP haploinsufficiency in mice results in tauopathy and cognitive deficits ameliorated by davunetide treatment. This article summarizes in brief recent reviews about NAP protection against tauopathy including the all D-amino acid analogue-D-NAP (AL-408). D-NAP was discovered to have similar neuroprotective functions to NAP in vitro. Here, D-NAP was tested as prophylactic as well as therapeutic treatment for amytrophic lateral sclerosis (ALS) in the widely used TgN(SOD1-G93A)1Gur transgenic mouse model. Results showed D-NAP-associated prophylactic protection, thus daily treatment starting from day 2 of age resulted in a prolonged life course in the D-NAP-treated mice, which was coupled to a significant decrease in tau hyperphosphorylation. These studies correlate protection against tau hyperphosphorylation and longevity in a severe model of ALS-like motor impairment and early mortality. NAP is a first-in-class drug candidate/investigation compound providing neuroprotection coupled to inhibition of tau pathology. D-NAP (AL-408) is a pipeline product.

摘要

达文肽(NAP)是一种针对 tau 病的领先候选药物。达文肽是一种八肽片段,通过对活性依赖性神经保护蛋白(ADNP)的结构活性研究衍生而来。ADNP 对大脑形成至关重要。ADNP 单倍不足的小鼠会导致 tau 病,并通过达文肽治疗得到改善。本文简要总结了近期关于 NAP 对 tau 病的保护作用的综述,包括全 D-氨基酸类似物-D-NAP(AL-408)。研究发现,D-NAP 在体外具有与 NAP 相似的神经保护功能。在这里,D-NAP 被测试为预防和治疗肌萎缩侧索硬化症(ALS)的方法,在广泛使用的 TgN(SOD1-G93A)1Gur 转基因小鼠模型中进行了测试。结果表明 D-NAP 具有预防保护作用,因此从出生后第 2 天开始每天进行治疗,可使 D-NAP 治疗的小鼠寿命延长,tau 过度磷酸化显著减少。这些研究在严重的 ALS 样运动障碍和早期死亡率模型中,将 tau 过度磷酸化的保护作用与寿命延长相关联。NAP 是一种首创的候选药物/研究化合物,可提供神经保护并抑制 tau 病理学。D-NAP(AL-408)是一种管线产品。

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